Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs264891608
- Species
- Mus musculus
- Symbol
- rs264891608
- Category
- Variant
- Variant type
- SNP
- Overlaps
- 1700001K19Rik
- Location
- 12:110648031
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)12:110648031G>A
- HGVS.c name
- ENSEMBL:ENSMUST00000070659.1:c.-128+974C>T
- ENSEMBL:ENSMUST00000222915.1:c.-92+974C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr12:110634122...110649053 (14.93 kb)
- Assembly version
- Not Available
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